Canonical Allele Identifier: CA657447855
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157638_55157639insA , CM000681.2:g.55157638_55157639insA GRCh38
NC_000019.9:g.55669006_55669007insA , CM000681.1:g.55669006_55669007insA GRCh37
NC_000019.8:g.60360818_60360819insA NCBI36
NG_007866.2:g.5094_5095insT , LRG_432:g.5094_5095insT
NG_032759.1:g.14084_14085insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.-50_-49insT MANE Select ENSP00000341838.5:n.-50_-49insT
ENST00000665070.1:c.-50_-49insT ENSP00000499482.1:n.-50_-49insT
ENST00000344887.9:c.-50_-49insT ENSP00000341838.5:n.-50_-49insT
ENST00000586446.1:n.94_95insT
ENST00000587176.5:n.135_136insT
ENST00000587871.1:c.571_572insT
ENST00000590463.1:n.78_79insT
NM_000363.4:c.-50_-49insT , LRG_432t1:c.-50_-49insT NP_000354.4:n.-50_-49insT
NM_000363.5:c.-50_-49insT MANE Select NP_000354.4:n.-50_-49insT